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FDA 510(k)

YTTRO FILTER

K-Number: K833779 · 1984-06-05

ApplicantYttro Corp.
Decision Date1984-06-05
Product CodeIZW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

YTTRO FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Yttro Corp.. It received FDA 510(k) clearance on 1984-06-05 under 510(k) number K833779. The device is classified under product code IZW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YTTRO FILTER?

YTTRO FILTER is a medical device that received FDA 510(k) clearance on 1984-06-05. The listed applicant is Yttro Corp.. The 510(k) number is K833779.

When did YTTRO FILTER receive FDA 510(k) clearance?

YTTRO FILTER received FDA 510(k) clearance on 1984-06-05, under 510(k) number K833779.

Who is the listed applicant for YTTRO FILTER?

The FDA 510(k) record lists Yttro Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YTTRO FILTER?

The FDA product code for YTTRO FILTER is IZW.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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